| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:812197-812699 | Common:6; Rare:173 | ||||
| chr18:812807-813019 | Common:1; Rare:52 | ||||
| chr18:2570749-2570909 | Common:1; Rare:31 | ||||
| chr18:2570962-2571087 | Common:2; Rare:20 | ||||
| chr18:2571371-2571651 | Common:1; Rare:73 | ||||
| chr18:2655464-2656073 | Common:6; Rare:226 | ||||
| chr18:2656232-2656375 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:2846866-2847102 | Rare:56 | ||||
| chr18:2847322-2847507 | Common:3; Rare:57 | ||||
| chr18:2906059-2906278 | Common:1; Rare:72 | ||||
| chr18:2906722-2907140 | Common:5; Rare:151 | ||||
| chr18:2982685-2982979 | Common:2; Rare:59 | ||||
| chr18:3012880-3012961 | Rare:23 | ||||
| chr18:3013082-3013394 | Common:3; Rare:118 | ||||
| chr18:3247035-3247426 | Common:5; Rare:97 |